Baobab Index

A database of publications about African genetic resources and digital sequence information — real bibliographic metadata pulled from PubMed, with a durable link back to the source record. Full text is frequently paywalled even when the abstract/metadata is open, so this is a metadata catalog with an outbound link, not a hosted archive; this platform never claims to host or redistribute full text.

curl "https://<hub-domain>/api/v1/publications"

Kaposi Sarcoma-Associated Herpesvirus Is Not Detected in Osteosarcoma From KSHV-Endemic African Countries and the Non-Endemic United States Populations.

Musonda W, Escalante GM, Liang Y, Bardin R, Barasa A, Geel J, Mumba C, Munsaka S, Munthali J, Reidel IG, Ogembo JG · J Med Virol (2026)

Zambia · DOI: 10.1002/jmv.71136

Osteosarcoma is an aggressive primary malignant bone tumor of poorly defined etiology that predominantly affects adolescents and young adults. A viral cause has long been proposed, and a recent study from Xinjiang, China, reported frequent detection of Kaposi sarcoma-associated herpesvirus (KSHV) in Uyghur osteosarcoma cases, suggesting a possible association in this KSHV-endemic population. Whether this association extends to broader populations remains unknown. Our study investigated the presence of KSHV in osteosarcoma specimens from KSHV-endemic African countries (Cameroon, Kenya, South Africa, Zambia) and the non-endemic United States. A total of 356 formalin-fixed paraffin-embedded and fresh-frozen specimens were retrieved or prospectively collected. In 77 selected high-quality specimens, KSHV infection was assessed by immunohistochemistry for LANA1 and by qPCR targeting 5 viral open reading frames (ORF25, ORF26, ORF37, ORF65, and ORF73). LANA1 expression was undetectable in all tumors. Using qPCR, 75/77 specimens were negative for all targets, 1/77 excluded due to insufficient remaining DNA quantity to perform the assay, and 1/77 positive across all five targets. Additionally, we studied the KSHV seroprevalence in a separate cohort comprised of 49 sera obtained from individuals with osteosarcoma from Zambia (n = 39) and the United States (n = 10). We measured by ELISA the presence of specific antibodies against four KSHV antigens: K8.1, KCP, VCA, and LANA1. KSHV seropositivity was detected in 15/39 individuals from Zambia and none from the United States. In the absence of compelling evidence, our findings could not support an association between KSHV infection and osteosarcoma in our study population.

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Integrating Cervical Cancer Prevention into HIV Services in Sub-Saharan Africa: A Narrative Review Addressing the Dual Burden Among Women.

Ceesay E, Avala Ntsigouaye J, Onwuka JU, Shanshan Y, Sokale IO, Gupta R, Okeke M, Okiemy EK, Bojang KS, Belec L · Open Forum Infect Dis (2026)

Gambia · DOI: 10.1093/ofid/ofag509

Women with HIV face a higher risk of cervical cancer. This review synthesizes evidence on precancerous cervical lesions among women with HIV in sub-Saharan Africa (SSA), regional differences, risk factors, and approaches to integrating cervical cancer prevention into HIV services. We conducted a comprehensive literature search across PubMed, Embase, Scopus, and Web of Science databases through December 2025 and identified studies evaluating the prevalence of precancerous cervical lesions among women with HIV in SSA. It highlights prevalence, ongoing global efforts, and integration strategies specific to SSA. The prevalence of precancerous cervical lesions among women with HIV in SSA is higher in Tanzania (71.8%), and Kenya (42%), eastern countries than from western (Nigeria, 26.6%) or southern countries (South Africa, 23.2%), influenced by the distribution of human papillomavirus (HPV) genotypes, including higher-risk HPV (HR-HPV) such as HPV 35, which is not targeted by the HPV vaccine. Given the increased risk among women with HIV and the substantial burden in SSA, evidence suggests that integrating HPV-based cervical cancer screening and vaccination into HIV care platforms could help close the prevention gap and reduce the dual burden among women with HIV in SSA.

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Ecological and methodological insights from genetic and coprological profiling of gastrointestinal communities in wild howler monkeys.

Carboni S, Macfarland C, Cheves Hernandez S, Buret AG, Kutz S, Melin AD · Sci Rep (2026)

Liberia · DOI: 10.1038/s41598-026-57628-6

The gastrointestinal tract hosts a complex community of microorganisms and helminth parasites that collectively contribute to host health and fitness. Analysis of these communities provides insight into diverse aspects of host dietary ecology, immunity, nutrition, and host-parasite interactions. However, research methodologies, such as sample preservation and sequencing approach, can influence how we understand and characterize these features. Here, we profiled the gastrointestinal microbial and helminth communities in different groups of wild Costa Rican mantled howler monkeys (Alouatta palliata palliata). We compared samples stored in ethanol versus directly flash frozen, and contrasted conclusions drawn from 16S versus shotgun sequencing approaches. Bacterial, archaeal, and eukaryotic taxa associated with the digestion of plant material dominated the GI communities. Storage and sequencing methods influenced microbial profiles: ethanol-stored samples exhibited higher diversity than frozen samples, and 16S sequencing detected lower diversity than shotgun. Helminths were detected via coprological microscopy in 71% of individuals, whereas metagenomic detection was inconsistent. This study provides new data on the microorganisms and their putative digestive functions in the gut of a folivorous primate, and highlights the pros and cons of different methodological choices when profiling host-microbiome and host-parasite interactions.

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Translating Flood-Tolerance Biology into Breeding: A 5D Framework for Next-Generation Rice Varieties.

Hussain W, Anumalla M, Zhang X, Ismail AM · J Exp Bot (2026)

Kenya · DOI: 10.1093/jxb/erag452

Flooding is among the most devastating abiotic stresses limiting rice productivity. Although SUB1A introgression conferred submergence tolerance in several mega-varieties, this single-gene approach is insufficient for the diverse flood types-flash floods, stagnant floods, anaerobic germination, and deepwater inundation-progressively intensifying with climate change. Here, we review the physiological mechanisms and genetic architecture underlying tolerance to each flood type, emphasizing the dual role of reactive oxygen species (ROS) in signalling and damage, the management of elemental toxicities (Fe2+, Mn2+) under altered soil redox, and lessons from wetland species and lowland rice. We then examine why marker-assisted selection has failed for polygenic, multi-stress tolerance and identify persistent breeding bottlenecks. Building on this biological foundation, we outline an integrated 5D framework (Demand, Discovery, Design, Development, Deployment) that links gene-bank diversity, multi-omics discovery, predictive breeding and on-farm validation through continuous feedback. We discuss how connected breeding, the transition-from-trait-to-environment (TTE) strategy, and speed breeding can accelerate genetic gain, and we close with research priorities centred on the biology of multi-flood tolerance to develop climate-resilient rice.

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Editorial: Sequencing technologies in advancing veterinary and zoonotic infection research.

Kariithi HM, Carabetta VJ, Leyson CL, Goraichuk IV · Front Cell Infect Microbiol (2026)

Kenya · DOI: 10.3389/fcimb.2026.1950388

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Harnessing Probiotic LAB and Bacteriocins for Clean-Label Food Processing and Biopreservation: Omics, Molecular Innovations and Industrial Applications.

Anumudu CK, Uhegwu CC, Çelen T · Probiotics Antimicrob Proteins (2026)

Nigeria · DOI: 10.1007/s12602-026-11201-9

The persistence of microbial agents in foods, especially spore forming bacteria is one of the most significant challenges to food preservation and safety, undermining product quality, shelf life, and consumer health. The use of traditional control methods, including thermal processing and chemical preservatives, are increasingly limited by consumer demands for minimally processed foods, and the emergence of resistant microbial strains. Advances have been made in the use of probiotics like lactic acid bacteria (LAB) and their biometabolites like bacteriocins in food processing and preservation, particularly to control biofilm and endospore forming pathogens including Bacillus sp., Listeria sp., Staphylococcus sp., Clostridium sp., E. coli etc. in foods and food processing plants/surfaces. Given the ability of these organisms to cause foodborne illness and form resilient biofilms in the food processing ecosystem and their resistance to the conventional method of their elimination, the antimicrobial peptides (bacteriocins) are gaining increasing prominence as useful alternatives to synthetic antimicrobials in enhancing food safety and combating the threats of these pathogens. This review addresses current information on the inhibition of persistent microbial spoilage contaminants, biofilm-forming pathogens, and spore formers of interest to the food industry using LAB and their bacteriocins. Current developments in isolation, characterization, and mode of action of bacteriocins are explored, including synergistic activity with other preservative hurdle techniques such as encapsulation, and nanobiotechnology. Importantly, there is a focus on the utilization of molecular and omics-based approaches to enable a better understanding of bacteriocin biosynthesis, gene regulation, host-microbe interactions and gut microbiome regulation potential of probiotic LABs, permitting the rational development of targeted and strain-specific interventions. Developments in the incorporation of bacteriocin-producing LAB into functional starter cultures and bio-protective products, and challenges in stability, regulatory approval, and scalability for industrial use, are also discussed in the paper. Despite their considerable potential, broader translation remains constrained by regulatory requirements, production and formulation costs, variable efficacy in complex food matrices, and the limited validation of many candidate bacteriocins beyond laboratory and model-food systems. Collectively, these advances position LAB and their bacteriocins at the leading edge of developing sustainable, clean-label, and efficacious functional foods and food preservation systems. Their functionality can be expanded by integrating genomics, synthetic biology, and predictive modeling for the maximization of their biopreservative potential in diverse food matrices and in gut microbiota modulation.

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publicrestrictedAFDSI-PUB-1013

Genomic dimensions deconstruct the clinical heterogeneity of bipolar disorder.

van der Veen T, Tesfaye M, Yang JMK, Boltz T, David FS, Crinion S, Koromina M, Andlauer TFM, Bigdeli TB, Coombes BJ, Greenwood TA, Panagiotaropoulou G, Parker N, Sung H, Bass N, Coleman JRI, Guzman-Parra J, Kalman JL, McGrouther CC, Mitchell BL, Rangan AV, Scott K, Shadrin A, Smith DJ, Vreeker A, Adorjan K, Albani D, Alemany S, Alliey-Rodriguez N, Antoniou A, Bauer M, Beins EC, Boks MP, Bosch R, Brumpton BM, Brunkhorst-Kanaan N, Budde M, Byerley W, Cabana-Domínguez J, Cairns MJ, Carpiniello B, Casas M, Cervantes P, Chatzinakos C, Clarke TK, Claus I, Cruceanu C, Cuellar-Barboza A, Czerski PM, Dafnas K, Dale AM, Dalkner N, DePaulo JR, Degenhardt F, Djurovic S, Escott-Price V, Fanous AH, Fellendorf FT, Ferrier IN, Forty L, Frank J, Frei O, Freimer NB, Garnham J, Gizer IR, Gordon SD, Gordon-Smith K, Hahn T, Hamshere ML, Harder A, Hautzinger M, Heilbronner U, Hellgren D, Herms S, Hickie IB, Hoffmann P, Holmans PA, Jamain S, Jonsson L, Kennedy JL, Kittel-Schneider S, Knowles JA, Koch E, Kogevinas M, Kranz TM, Kushner SA, Lavebratt C, Lawrence J, Leber M, Lind PA, Lucae S, Lundberg M, MacIntyre DJ, Maier W, Maihofer AX, Malaspina D, Manchia M, Maratou E, Martinsson L, McInnis MG, McKay JD, Medeiros H, Meyer-Lindenberg A, Millischer V, Morris DW, Moutsatsou P, Mühleisen TW, O'Donovan C, Olsen CM, Papiol S, Pardiñas AF, Perry A, Pfennig A, Pisanu C, Potash JB, Quested D, Rapaport MH, Regeer EJ, Rice JP, Rivera M, Schulte EC, Senner F, Shilling PD, Sindermann L, Sirignano L, Siskind D, Slaney C, Smeland OB, Sobell JL, Artigas MS, Stein DJ, Stein F, Swiatkowska B, Thorp JG, Toma C, Tondo L, Tooney PA, Vawter MP, Vedder H, Walters JTR, Witt SH, Young AH, Zandi PP, Zillich L, Estonian Biobank research team, Genomic Psychiatry Cohort (GPC) Investigators, HUNT All-In Psychiatry, Adolfsson R, Alfredsson L, Backlund L, Baune BT, Bellivier F, Bengesser S, Berrettini WH, Biernacka JM, Blackwood D, Boehnke M, Breen G, Carr VJ, Catts S, Cichon S, Corvin A, Craddock N, Dannlowski U, Dikeos D, Esko T, Etain B, Ferentinos P, Frye M, Fullerton JM, Gawlik M, Gershon ES, Goes FS, Green MJ, Hauser J, Henskens FA, Hjerling-Leffler J, Jones I, Jones LA, Kahn RS, Kelsoe JR, Kircher T, Kirov G, Kobayashi N, Landén M, Leboyer M, Lenger M, Li QS, Lissowska J, Loughland C, Luykx JJ, Martin NG, Mathews CA, Mayoral F, McElroy SL, McIntosh AM, Medland SE, Melle I, Mitchell PB, Morken G, Myers RM, Möser C, Müller-Myhsok B, Neale BM, Nievergelt CM, Nurnberger JI, Nöthen MM, O'Donovan MC, Oedegaard KJ, Olsson T, Owen MJ, Paciga SA, Pantelis C, Pato CN, Pato MT, Patrinos GP, Pawlak JM, Perlis R, Ramos-Quiroga JA, Reif A, Reininghaus EZ, Ribasés M, Rietschel M, Ripke S, Rouleau GA, Schall U, Schalling M, Schofield PR, Schulze TG, Scott LJ, Scott RJ, Serretti A, Smoller JW, Squassina A, Stahl EA, Stordal E, Streit F, Sullivan PF, Turecki G, Vaaler AE, Vieta E, Vincent JB, Waldman ID, Weickert CS, Weickert TW, Whiteman DC, Alda M, Ophoff RA, O'Connell KS, Mullins N, Forstner AJ, Grigoroiu-Serbanescu M, Edenberg HJ, McMahon FJ, Andreassen OA, Di Florio A, McQuillin A · Res Sq (2026)

South Africa · DOI: 10.21203/rs.3.rs-10041361/v1

Bipolar disorder's (BD) clinical heterogeneity has an unresolved genetic basis. We meta-analyzed genome-wide association studies (GWAS) of 16 BD subphenotypes in 226,032 individuals from 57 cohorts (38,022 cases); 10 advanced to multivariate and multi-trait analyses. Four factors (compulsive, psychotic, dysregulated, internalizing) explained 82.8% of shared genetic variance. BD1 and BD2 loaded on distinct factors despite a high genetic correlation; 87.0% of common-factor loci were significant in neither subtype. Unipolar mania aligned with psychosis over internalizing, and was distinguishable from BD1, and rapid cycling showed heritable cross-domain liability. We identified 356 risk loci, 158 novel, including the first univariate-GWAS associations for psychosis, unipolar mania, rapid cycling and schizoaffective disorder-and 249 credible genes (89 high-confidence), 12 with approved-drug or clinical-phase annotations. Cell-type association showed a midbrain dopaminergic-GABAergic gradient along the psychotic factor. BD's genetic architecture appears hierarchical-a general liability resolving into dimensions of course and comorbidity, beyond subtypes.

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Tracing the evolution and diversity of human parvovirus B19 across human history.

Zeibig T, Spyrou MA, Kocher A, Gaul E, Aldenderfer M, Barquera R, Beckett JF, Beisenov A, Belinski AB, Betancourt PP, Boersma R, Carrion P, Childebayeva A, Cooper C, Cucca F, Di Salvo R, Dizdar M, Djansugurova L, Ernée M, Ferrence SC, Fehren-Schmitz L, Ghalichi A, Giffin KL, Gilbert S, Gómez-Valdés JA, Gretzinger J, Hansen L, Hansen S, Hernandez-Zaragoza DI, Jankauskas R, Jeong C, Keller M, Khartanovich V, Kim D, Kinaston R, Kovalev A, Kozakaitė J, Krausse D, Krznar S, Küßner M, Langford LC, Lai L, Lösch S, Majander K, Mannino MA, Márquez-Morfín L, McCormick M, McGeorge PJP, Michel M, Moiseyev V, Moon H, Mötsch A, Musralina L, Myagmar E, Nakoro E, Németh RE, Neumann GU, Novak M, Olmo Enciso L, Onkamo P, Papac L, Peltola S, Posth C, Powell A, Radimilahy C, Rajković D, Rakotoarisoa JA, Rasoarifetra BN, Reinhold S, Risch R, Samashev Z, Sayer D, Schimmenti V, Schmitt F, Sintes E, Slavin P, Sorokin D, Terberger T, Tukhbatova R, Vågene ÅJ, Van de Vijver K, Vigil-Escalera Guirado A, Villalba-Mouco V, Voyakin D, Woo EJ, Ximenez T, Stockhammer P, Warinner C, Bos K, Schiffels S, Mittnik A, Haak W, Herbig A, Krause J · Curr Biol (2026)

Madagascar · DOI: 10.1016/j.cub.2026.08.032

Human parvovirus B19 (B19V) is an ubiquitously spread, exclusively human pathogen, mainly posing risks to children, as well as pregnant and immunocompromised individuals. Despite evidence of B19V infection of human populations as far back as 7,000 years, the evolutionary history of B19V remains poorly understood. In this study, we present B19V genomic data from the remains of 53 globally distributed individuals spanning more than 8,000 years, including 7 children. Our findings suggest that the most recent common ancestor of all present B19V lineages existed around 12,000 years ago, at the end of the last Ice Age. Additionally, we identified an extinct Eurasian clade that participated in the recombination event that led to the emergence of B19V genotype 2 (GT-2). We date this event to ∼3,200-1,800 BP, potentially in the greater Mediterranean area. Our study shows aspects of how ancient parvovirus variants arose, disseminated, and impacted human health through time.

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publicrestrictedAFDSI-PUB-1011

Functional validation of the Plasmodium falciparum K13 C580Y mutation in recently collected Ethiopian isolates.

Mukherjee A, Assefa AB, Turlo CV, Needham LC, Shoue D, Qahash T, Belachew M, Tadesse D, Kassie E, Berihun M, Brhane BG, Parr JB, Ferdig MT, MAREE Consortium · Antimicrob Agents Chemother (2026)

Ethiopia · DOI: 10.1128/aac.00495-26

Recent genomic investigation in Ethiopia identified the first detection of the

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publicrestrictedAFDSI-PUB-1010

Holistic approaches for improvement of maize resistance against lodging stress: current status and future perspective.

Getachew G, Deressa T, Runo S · Mol Genet Genomics (2026)

Ethiopia · DOI: 10.1007/s00438-026-02465-5

Lodging is a major constraint in maize production, causing significant yield losses, reduced grain quality, and harvesting inefficiencies, thereby posing a serious challenge to global food security and climate-resilient agriculture. This review synthesizes current knowledge on the genetic, physiological, and agronomic determinants of maize lodging resistance and evaluates holistic strategies for improving tolerance to lodging stress. Recent advances in quantitative trait locus (QTL) mapping, genome-wide association studies (GWAS), functional gene characterization, genome editing, high-throughput phenotyping, and precision agronomy have provided powerful tools to enhance stalk biomechanics, root anchorage, and adaptive plant architecture. Integrating genomic discovery with advanced phenomics and optimized agronomic management offers a scalable framework for accelerating the development of high-yielding, lodging-resilient maize cultivars. However, critical gaps remain in understanding the genetic coordination between stalk strength and root system architecture, integrating multi-omics approaches to unravel regulatory networks, validating genome-editing interventions across diverse agro-ecologies, and developing environment-responsive predictive breeding models and cost-effective phenotyping tools, particularly for stress-prone regions. Addressing these challenges through coordinated multi-environment trials and integrative molecular-agronomic strategies will facilitate the translation of genomic discoveries into climate-resilient, high-performing maize cultivars. By consolidating molecular insights with applied breeding and management practices, this review provides a comprehensive framework that guides researchers in designing genome-informed and field-validated approaches to improve maize resistance to lodging stress and support sustainable crop production systems.

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